Der renale Phänotyp beim Very-Long-Chain Acyl-CoA Dehydrogenase- (VLCAD-) Mangel: Studien am VLCAD-/--Mausmodell
- Alternative title
-
The renal phenotype in very-long-chain Acyl-CoA Dehydrogenase- (VLCAD-) Deficiency: Studies on the VLCAD-/--mouse model.
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Language
-
Deutsch
- Notes
-
Düsseldorf, Heinrich-Heine-Universität, Dissertation, 2020
- Keyword
-
Acyl-Coenzym-A-Dehydrogenase
Fettsäuren
Levocarnitin
Phänotyp
- Event
-
Veröffentlichung
- (where)
-
Düsseldorf
- (who)
-
Universitäts- und Landesbibliothek der Heinrich-Heine-Universität Düsseldorf
- (when)
-
2020
- Creator
-
Krogmann, Antonia
- Contributor
- URN
-
urn:nbn:de:hbz:061-20200902-110942-3
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:55 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Krogmann, Antonia
- Spiekerkötter, Ute
- Keitel- Anselmino, Verena
- Universitäts- und Landesbibliothek der Heinrich-Heine-Universität Düsseldorf
Time of origin
- 2020
Other Objects (12)
Entzugsphänomene beim Absetzen von Phenobarbital und Primidon : wovon sind sie abhängig?
Triheptanoin: long-term effects in the very long-chain acyl-CoA dehydrogenase-deficient mouse
Sex‐specific perturbation of complex lipids in response to medium‐chain fatty acids in very long‐chain acyl‐CoA dehydrogenase deficiency
Modification of dietary substrates impacts glucose homeostasis in very long-chain Acyl-CoA dehydrogenase deficient (VLCAD-/-) mice
Charakterisierung Neugeborener mit dem Verdacht eines Medium- chain acyl- CoA Dehydrogenase (MCAD)- Mangels im Screening
Medium-chain acyl-CoA dehydrogenase deficiency associated with a novel splice mutation in the ACADM gene missed by newborn screening
Medium-chain acyl-CoA dehydrogenase deficiency associated with a novel splice mutation in the ACADM gene missed by newborn screening
Korrelation der Methylmalonsäurekonzentration im Urin und der Entwicklung einer chronischen Niereninsuffizienz bei Kindern mit Methylmalonazidurie
Untersuchungen zur Lebensqualität von Kindern mit Phenylketonurie
The phenotypic and genetic spectrum of glycogen storage disease type VI
Severe loss of appetite and refusal to eat as severe side effect of glycerol phenylbutyrate
Reversible sensory neuropathy in mitochondrial trifunctional protein deficiency
Entzugsphänomene beim Absetzen von Phenobarbital und Primidon : wovon sind sie abhängig?
Triheptanoin: long-term effects in the very long-chain acyl-CoA dehydrogenase-deficient mouse
Sex‐specific perturbation of complex lipids in response to medium‐chain fatty acids in very long‐chain acyl‐CoA dehydrogenase deficiency
Modification of dietary substrates impacts glucose homeostasis in very long-chain Acyl-CoA dehydrogenase deficient (VLCAD-/-) mice
Charakterisierung Neugeborener mit dem Verdacht eines Medium- chain acyl- CoA Dehydrogenase (MCAD)- Mangels im Screening
Medium-chain acyl-CoA dehydrogenase deficiency associated with a novel splice mutation in the ACADM gene missed by newborn screening
Medium-chain acyl-CoA dehydrogenase deficiency associated with a novel splice mutation in the ACADM gene missed by newborn screening
Korrelation der Methylmalonsäurekonzentration im Urin und der Entwicklung einer chronischen Niereninsuffizienz bei Kindern mit Methylmalonazidurie
Untersuchungen zur Lebensqualität von Kindern mit Phenylketonurie
The phenotypic and genetic spectrum of glycogen storage disease type VI
Severe loss of appetite and refusal to eat as severe side effect of glycerol phenylbutyrate
Reversible sensory neuropathy in mitochondrial trifunctional protein deficiency
Entzugsphänomene beim Absetzen von Phenobarbital und Primidon : wovon sind sie abhängig?
Triheptanoin: long-term effects in the very long-chain acyl-CoA dehydrogenase-deficient mouse
Sex‐specific perturbation of complex lipids in response to medium‐chain fatty acids in very long‐chain acyl‐CoA dehydrogenase deficiency
Modification of dietary substrates impacts glucose homeostasis in very long-chain Acyl-CoA dehydrogenase deficient (VLCAD-/-) mice
Charakterisierung Neugeborener mit dem Verdacht eines Medium- chain acyl- CoA Dehydrogenase (MCAD)- Mangels im Screening
Medium-chain acyl-CoA dehydrogenase deficiency associated with a novel splice mutation in the ACADM gene missed by newborn screening
Medium-chain acyl-CoA dehydrogenase deficiency associated with a novel splice mutation in the ACADM gene missed by newborn screening
Korrelation der Methylmalonsäurekonzentration im Urin und der Entwicklung einer chronischen Niereninsuffizienz bei Kindern mit Methylmalonazidurie
Untersuchungen zur Lebensqualität von Kindern mit Phenylketonurie
The phenotypic and genetic spectrum of glycogen storage disease type VI
Severe loss of appetite and refusal to eat as severe side effect of glycerol phenylbutyrate